Foaming Instant Hand Sanitizer
- Product NDC
- 78641-207
- Requested package NDC
- 78641-207-78
- 11-digit product format
- 786410207
- Labeler code
- 78641
- Product ID
- 78641-207_d6e40ab7-56d9-0af7-e053-2995a90a1c8e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Global Equipment Company
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-16
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 78641-207-78 | 78641020778 | 950 mL in 1 BOTTLE (78641-207-78) | 950 ml | 2020-03-16 | 0000-00-00 | No | No | Current |